methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate

Base Information

• Chemical Name: methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate
• CAS No.: 165529-15-7
• Molecular Formula: C₂₅H₃₂N₂O₄
• Molecular Weight: 424.54

Synonyms:methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate

Chemical Property of methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate

Chemical Property:

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Technology Process of methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate

There total 5 articles about methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

methyl N-[2-amino-4-(t-butoxycarbonyl)benzyl]-N-phenylethyl-4-aminocrotonate (165529-14-6) → methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate (165529-15-7)

Guidance literature:

In methanol;

Reference yield:

2-nitro-4-(tert-butoxycarbonyl)benzyl bromide (65276-90-6) → methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate (165529-15-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 88 percent / Et₃N / tetrahydrofuran / 16 h / Ambient temperature

2: Fe, AcOH / ethanol / 16 h / Ambient temperature

3: methanol / 72 h / Heating

With iron; acetic acid; triethylamine; In tetrahydrofuran; methanol; ethanol;

DOI:10.1021/jm980166z

Reference yield:

4-phenethylaminocrotonate → methyl (R,S)-8-(t-butoxycarbonyl)-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate (165529-15-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 88 percent / Et₃N / tetrahydrofuran / 16 h / Ambient temperature

2: Fe, AcOH / ethanol / 16 h / Ambient temperature

3: methanol / 72 h / Heating

With iron; acetic acid; triethylamine; In tetrahydrofuran; methanol; ethanol;

DOI:10.1021/jm980166z

upstream raw materials:

2-nitro-4-(tert-butoxycarbonyl)benzyl bromide

4-{[(3-methoxycarbonyl-allyl)-phenethyl-amino]-methyl}-3-nitro-benzoic acid tert-butyl ester

methyl N-[2-amino-4-(t-butoxycarbonyl)benzyl]-N-phenylethyl-4-aminocrotonate

Downstream raw materials:

methyl (R,S)-8-[[[4-[N-(t-butoxycarbonyl)aminoiminomethyl]phenyl]amino]carbonyl]-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate

[8-(4-carbamimidoyl-phenylcarbamoyl)-4-phenethyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepin-2-yl]-acetic acid methyl ester

methyl (R,S)-8-carboxy-2,3,4,5-tetrahydro-4-(2-phenylethyl)-1H-1,4-benzodiazepine-2-acetate

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